Bridging the Laboratory and Your Market
Confab will expedite your drug development program through effective, efficient production of clinical trial materials. Our formulation scientists and manufacturing teams work directly with you and/or your contract research organization (CRO) to assist with technology transfers for later-phase clinical trial materials, registration batches and commercial launch.
- Phase I-III registration batches and commercial launch
- cGMP batch sizes from 10kg
- Extensive packaging capabilities
To simplify your pathway to approval, we provide regulatory submission support, such as chemistry, manufacturing and control (CMC) services for investigational new drug (IND) applications. And our regulatory and clinical trial manufacturing teams work closely to ensure efficient, accurate submission of a detailed CMC filing for the IND.
Confab has extensive capabilities in clinical trial manufacturing and can help with identification of packaging options, compatibility assessment and other related tasks. Also, our experts with decades of scale-up experience can provide estimates for when a product begins commercial cGMP manufacturing.